Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia.

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作者： Anna,Alkelai ^[1] ; Shahar,Shohat ^[2] ; Lior,Greenbaum ^[3] ; Tanya,Schechter ^[4] ; Benjamin,Draiman ^[5] ; Eti,Chitrit-Raveh ^[6] ; Shlomit,Rienstein ^[6] ; Neha,Dagaonkar ^[6] ; Daniel,Hughes ^[3] ; Vimla S,Aggarwal ^[7] ; Erin L,Heinzen ^[7] ; Sagiv,Shifman ^[7] ; David B,Goldstein ^[7] ; Yoav,Kohn ^[8]

作者单位： Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA. aa3857@cumc.columbia.edu. ^[1] Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel. ^[2] The Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel Hashomer, Israel. ^[3] The Joseph Sagol Neuroscience Center, Sheba Medical Center, Tel Hashomer, Israel. ^[4] Sackler Faculty of Medicine, Tal Aviv University, Tel Aviv, Israel. ^[5] Department of Child and Adolescent Psychiatry, Jerusalem Mental Health Center, Eitanim Psychiatric Hospital, Jerusalem, Israel. ^[6] Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA. ^[7] Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA. ^[8] Hadassah-Hebrew University School of Medicine, Jerusalem, Israel. ^[9]